Canonical Allele Identifier: CA1742564296
Gene: FLNC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.128849379C= , CM000669.2:g.128849379C= GRCh38
NC_000007.13:g.128489433C= , CM000669.1:g.128489433C= GRCh37
NC_000007.12:g.128276669C= NCBI36
NG_011807.1:g.23951C= , LRG_870:g.23951C=

Transcript Alleles

HGVS Amino-acid change
ENST00000325888.13:c.5000C= MANE Select ENSP00000327145.8:p.Thr1667=
ENST00000325888.12:c.5000C= ENSP00000327145.8:p.Thr1667=
ENST00000346177.6:c.5000C= ENSP00000344002.6:p.Thr1667=
NM_001127487.1:c.5000C= NP_001120959.1:p.Thr1667=
NM_001458.4:c.5000C= , LRG_870t1:c.5000C= NP_001449.3:p.Thr1667=
NM_001127487.2:c.5000C= NP_001120959.1:p.Thr1667=
NM_001458.5:c.5000C= MANE Select NP_001449.3:p.Thr1667=